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A recent Effexor birth defect lawsuit filed by a Kentucky mother alleges that her son was born with heart and other abnormalities following her use of the SNRI antidepressant. The mother was prescribed the drug just a year before she conceived and continued it until her second trimester. She came to know about its potential side effects only a few years ago after a medical journal cited two-fold greater risk of heart and other birth defects associated with the drug pregnancy side effects, her Kentucky Effexor birth defect attorney claimed. Her doctor was not even aware of any Effexor birth defect risk in the absence of any such information by the manufacturer.
The first Effexor birth defect lawsuit was initiated by an Ohio couple in 2012 after research reports highlighted link between congenital lung, heart, brain, and other abnormalities and antidepressants. Until then, the drug was purchased by millions who were made to believe by the manufacturer that it was safer than SSRI and other medications with enhanced ability to treat patients suffering from depression.
The federal Effexor MDL has expanded manifold in the past three years with more and more mothers coming forward to file lawsuits. Effexor birth defect lawyers in Kentucky, Tennessee, Arkansas, and other states are now evaluating hundreds of claims citing “failure to warn, design defect, negligent design, fraud, breach of warranty, gross negligence, and violation of Consumer Sales Practices Acts.”
Studies Warn of Effexor Birth Defects
There are many research studies and clinical evaluations discovering a possible link between antidepressant pregnancy side effects and congenital deformities in newborns. These reports help a Kentucky Effexor birth defect attorney, plaintiffs, and consumer activists to identify the exact nature of injuries and relate it to antidepressant adverse impacts.
In 2002, a group of Australian researchers found that the antidepressant medication was prone to causing toxicity. Four years later, the New England Journal of Medicine warned of fatal lung disorder in newborn babies linked to Effexor. Known as Persistent Pulmonary Hypertension (PPHN), the disorders inhibits the function of lungs immediately after birth and results in acute circulatory distress.
A report endorsed by the Canadian Medical Association warned of two-fold threat of miscarriages following Effexor use. Published in 2010, it cautioned expectant mothers against taking the antidepressant except when benefits were expected to be worthy of such a risk. The FDA has also categorized the drug as Pregnancy C category, which means “risk not ruled out and animal reproduction studies have shown an adverse effect on the fetus, though there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.”
The American Academy of Pediatrics notified its members in 2012 of potential Effexor birth defects. According to the British Medical Journal, Effexor birth defects may include physical abnormalities, heart defects, and congenital deformities. Mothers may suffer from post-delivery bleeding while there is two-time higher threat of babies born with hypoplastic hearts.
A group of researchers from Denmark discovered that Effexor exposure during prenatal stage may lead to delayed development and growth in children. There are also reports of autism, spina bifida, and brain malformations associated with antidepressant pregnancy side effects.
Reported Effexor Birth Defects
According to Effexor birth defect lawsuits filed in the past three years, the antidepressant ingestion by pregnant woman caused babies born with
- heart defects, such as neonatal cardiac complications fused heart, septal holes, ventral abnormalities, defective valves
- lung disorders, such as PPHN and hypoplastic lungs
- circulatory problems and Fallot syndrome
- cranial problems, such as craniosynostosis, anencephaly, fused skull, brain malformations, and development delays
- club foot, cleft lip and palate
- infant death or surgery due to underdeveloped organs
There are many studies and claims being evaluated by our Effexor birth defect attorney in Kentucky claim damaged intestine, anus malformations, spinal defects, autism, deformed vertebra, abdominal large head, and various types of limb defects.
If your child is a victim of Effexor birth defect and you are willing pursue defective medical device product liability lawsuit seeking financial damages, please contact our experienced Effexor birth defect attorney in Kentucky or call on 1-800-632-1404 for a free consultation.
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